List of variants in gene FAT4 reported as likely benign for immune system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001291303.3(FAT4):c.14361C>T (p.Val4787=)	rs1014865	0.01862
NM_001291303.3(FAT4):c.8592G>A (p.Val2864=)	rs111758803	0.01583
NM_001291303.3(FAT4):c.1101A>G (p.Val367=)	rs57692448	0.01498
NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val)	rs142747281	0.00288
NM_001291303.3(FAT4):c.14935G>A (p.Ala4979Thr)	rs17009858	0.00011
NM_001291303.3(FAT4):c.4228G>A (p.Val1410Met)	rs781736766	0.00004
NM_001291303.3(FAT4):c.11039C>T (p.Thr3680Met)	rs367877267	0.00003
NM_001291303.3(FAT4):c.2824A>G (p.Ile942Val)	rs368138514	0.00001
NM_001291303.3(FAT4):c.3637G>T (p.Asp1213Tyr)	rs762595829	0.00001
NM_001291303.3(FAT4):c.842C>T (p.Thr281Ile)	rs564305264	0.00001

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